Evidence map›Paper›PMID 42802121›Full record

ArticleZhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology2026

[Expert recommendations on the first-line use and optimization plan of nucleos(t)ide analogues in the context of functional cure for chronic hepatitis B].

Liver Cancer Study Group, Chinese Society of Hepatology, Chinese Medical Association

Abstract readEnglish Abstract
In one paragraph

Article in Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

1 author.

Liver Cancer Study Group, Chinese Society of Hepatology, Chinese Medical Association

Funding

2024 Hebei Provincial Medical Applicable Technology Tracking Project GZ20240482024 In-Hospital Integrated Traditional Chinese and Western Medicine Research Project at Hebei Medical University Third Hospital [2024]19China Liver Health LetterThe Key Research and Development Program of Hebei Province-Biomedical Innovation Project 23377705D
6 · The paper itself

Abstract

Novel therapeutic approaches aimed at achieving a functional cure for chronic hepatitis B have become a hot topic of academic research. However, the optimal timing of antiviral therapy and selection of nucleos(t)ide analogues (NAs) for different patient populations with chronic HBV infection remain unclear in the context of clinics. Based on current guidelines and available clinical evidence, expert recommendations have been developed with a focus on the timing of antiviral therapy and strategies for optimizing NA treatment before novel therapies aimed at achieving a functional cure become clinically accessible: (1) Patient populations with chronic hepatitis B who may benefit from novel therapies aimed at achieving a functional cure include those with hepatitis B surface antigen (HBsAg) ≤3,000 IU/mL, HBV DNA <90 or 100 IU/mL, and alanine aminotransferase (ALT) ≤2× the upper limit of normal (ULN). (2) For HBV DNA-positive patients aged 18-30 with chronic HBV infection, antiviral therapy should be initiated early to maximize the reduction of risks for conditions such as cirrhosis and hepatocellular carcinoma associated with advanced aging. (3) For patients who are not expected to benefit from novel therapies aimed at achieving a functional cure, early initiation of NA therapy is recommended to promote their transition into a population that may benefit from it. (4) After a functional cure has been achieved, HBV infection status should be reevaluated before administering medications that have a risk of HBV reactivation to determine whether prophylactic NA therapy is needed.

Indexed as

Antiviral AgentsHepatitis B, ChronicNucleosidesNucleotidesHepatitis B virusHumansAntiviral AgentsNucleosidesNucleotides

Identifiers

PMID42802121
PMCPMC13616986

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.